Abstract: Systems and methods for analyzing the gait of an individual are disclosed. The disclosed systems and methods can be configured to acquire data from a first array and a second array of sensors that are configured to be placed in a left and/or right shoe, respectively. The acquired data can be collected or separated into at least two separate gait phases for each array, compared to a baseline condition for each gait phase and categorized into one of at least two uniformity categories for each gait phase. Examples of collected and/or calculated data include pressure values, shear stress values and torque values. The analysis can be focused on both feet of a person, or focused on one foot. A graphical output showing at least one entire gait cycle based on the uniformity categories can then be generated.

Abstract: A surgical instrument includes a movable member having a proximal portion, the movable member defining an opening at the proximal portion. The instrument includes a stationary member defining an aperture. The stationary member is arranged relative to the movable member with a close fit between the stationary member and the movable member such that aspiration occurs through the movable member substantially only during a portion of a repetitive motion of the movable member. The instrument includes a surgical handpiece coupled to the movable member and the stationary member to provide suction and motion to the movable member.

Abstract: A dive computer system that utilizes a direct skin temperature measurement is provided. The dive computer system includes a measurement device that includes a temperature sensor and is attached to a strap. The strap is placed around a diver's chest and configured to measure the diver's skin temperature. The skin temperature is wirelessly transmitted to a dive computer that utilizes a dive algorithm to determine compartment inert gas saturation and desaturation. The dive algorithm determines an updated skin perfusion factor that is in turn utilized to determine an updated half time for the skin compartment for inert gas desaturation and a pressure tolerance for the skin compartment for inert gas saturation.

Abstract: A flexible biopsy needle assembly includes a flexible coring stylet that is slidably disposed within a flexible outer cannula. The stylet includes an elongated body, a tip, a sampling notch adjacent to the tip, and at least one ferrule along the length of the body. The cannula includes an elongated tubular body defining a lumen sized for sliding passage of the stylet, a cutting edge at the opening of the lumen, and an array of slits along the length of its body. The slits are sized to allow the diameter of the ferrule(s) to extend partially therein. The slits and ferrule(s) interact to limit or control the flexibility of the cannula at the location of the slits.

Abstract: A device for measuring electromyographic signals 2 is adapted to receive, through multiple channels “C”, electromyographic signals “EMG” sensed by a plurality of electrodes 3 arranged on a patient “P”. The device 2 includes: a conditioning circuit 21; a conversion circuit 22; a transmission circuit 23 to transmit the digitalized signals to a central control unit 1; an external casing 20 to enclose the circuits (21, 22, 23). The conditioning circuit 21 can be assembled modularly by establishing a cascade connection of one or more conditioning circuits 21. The conversion circuit 22 can be assembled modularly by connecting in parallel one or more conversion circuits 22 to vary the number of channels “C” through which electromyographic signals “EMG” are received. The conditioning circuits 21 and the conversion circuits 22 overlap at least partially to limit the dimensions of the external casing 20, ensuring wearability on the patient “P”.

Abstract: A system and method for monitoring the health of an animal using multiple sensors is described. The wearable device may include one or more sensors whose resultant signal levels may be analyzed in the wearable device or uploaded to a data management server for additional analysis. In one example, paired thermometers are used to estimate a core temperature of the animal, with one of the thermometers facing inward toward the animal and the other thermometer facing away from the animal.

Abstract: Apparatus for allowing measurements to be made of a blood sample comprises a shaft and at least first and second blood collection members. The blood collection members are independently rotatable about the shaft. Each blood collection member includes: a blood analysis part for receiving a blood sample, plural conductive contacts, and plural conductors extending between the blood analysis part and respective ones of the conductive contacts. The apparatus also includes plural terminals configured to provide an electrical connection with the plural conductive contacts on a first member when the apparatus is in a first configuration and to provide an electrical connection with the plural conductive contacts on a second member when the apparatus is in a second configuration, thereby allowing successive measurements of at least one parameter of blood samples provided on the blood analysis parts of the first and second members.

Abstract: An embodiment of the present invention provides a kit of parts for use in a surgical procedure performed under image guidance, and particularly under real time image guidance. The kit includes a sterilized drape for use with the chosen imaging machine and which can be used to provide a sterile operating environment when the procedure is performed under the imaging beam. The kit also includes a needle holder that can keep the surgeon's hand away from the imaging beam. The needle holder is operable to hold a needle that is made from a material suitable for piercing tissue, but also substantially preserves the appearance of the needle when it is viewed under the imaging beam.

Abstract: A cryogenic biopsy device is configured to provide thin, frozen tissue samples, which may be viewed under a microscope and selected for biomarker analysis. The device is configured to provide slices which are less than 50 micrometers in thickness, while snap-freezing the tissue and maintaining the sample in a deep-frozen state until it reaches the pathology lab for further processing. Alternatively, thicker slices can be harvested by the device and additional sectioning can be done in the pathology lab by using cryomicrotome. The device of the present invention may be used in rigid instruments and in flexible devices, such as endoscopes, for example, and may be suitable for single use or multiple use.

Abstract: A tissue handling system includes a biopsy device having an invasive unit with tissue-receiving and tissue-severing components being capable of harvesting and bringing at least one tissue sample to a point outside the body of a patient. The tissue handling system further includes a tissue collecting device adapted to be brought in detachable operative engagement with the tissue-receiving components of the biopsy device to remove the at least one tissue sample. Additionally, the tissue handling device comprises a tissue storage container configured to receive the at least one tissue sample, the entire tissue collecting device, or the part of the collecting device that contains the at least one tissue sample. The tissue storage container further is configured to receive a volume of preserving agent. The tissue handling system also comprises a vessel including the preserving agent adapted to be gas-tightly mated or coupled to the tissue storage container.

Abstract: A biopsy system includes a biopsy targeting assembly, a needle, and a biopsy device. The biopsy targeting assembly includes a cradle. The needle is releasably supported by the targeting assembly. The biopsy device includes a body having a tissue collection assembly and a cutter. The cutter is translatable relative to the body and extends distally from the body. The cradle of the targeting assembly releasably supports the body of the biopsy device distally of the tissue collection assembly. The biopsy device translates a distal portion of the cutter within the needle with the needle supported by the targeting assembly.

Abstract: A blood testing apparatus includes a laser source configured to produce a wound from which blood flows and at least one test member. A humidity cover is positioned at the at least one test member. The humidity cover is at least partially removable. Electronics are provided for analysis. The electronics includes an evaluation device for comparisons with previously stored measurements or evaluation data with the evaluation device storing a current test measurement.

Abstract: A spinal probe comprises a handle, a shaft coupled to the handle and a force sensor to detect forces applied to a tip of the shaft. A controller that executes a predictive algorithm to predict whether or not the tip of the shaft is going to breach a cortex of a pedicle based on the detected forces. The controller may be embedded within the spinal probe or external within a computer or other device coupled to the probe by a data acquisition component.

Abstract: A medical guide wire which has a core wire having a distal end-side small-diameter portion and a proximal end-side large-diameter portion having a larger outside diameter than the outside diameter of the distal end-side small-diameter portion, and a coil spring installed on an outer periphery of the distal end-side small-diameter portion of the core wire along an axial direction and fixed to the core wire at at least the front end portion and rear end portion thereof. The outside diameter of the proximal end-side large-diameter portion of the core wire and the outside diameter of coil of the coil spring are each at most 0.012 inch. The front end portion of the coil spring is fixed to the core wire by gold-containing solder. The length of a distal end portion stiffened by the gold-containing solder is 0.1 to 0.5 mm. The medical guide wire is high in fixing strength of the coil spring to the core wire and can shorten a shaping length compared with a conventional medical guide wire.

Abstract: A blood separation and testing system for a blood sample is disclosed. The blood separation and testing system includes a blood sampling transfer device adapted to receive a blood sample, a blood separation device, and a blood testing device. The blood separation device is adapted to receive a portion of the blood sampling transfer device such that with the blood sampling transfer device received within the blood separation device and a rotational force applied to the blood sampling transfer device, a plasma portion of the blood sample is separated from a cellular portion of the blood sample. The blood testing device is adapted to receive a portion of the blood sampling transfer device to analyze the plasma portion of the blood sample and obtain test results.

Abstract: A method of monitoring relative nerve health and the presence of neuropraxia is described. The methods utilize the integration of a waveform function of an elicited or monitored nerve response to provide an indication of the strength of a detected signal from a nerve and thus the relative health and integrity of the nerve. In some embodiments motor nerve stimulation innervates muscle and an EMG waveform is obtained in response thereto. The integration under the waveform is expressed and an indexed value indicating a percentage of a certain threshold value. Methods set forth provide a more reliable status of a nerve in real-time and allow action to be taken to reduce neuropraxia or prevent permanent nerve damage.

Abstract: According to certain described aspects, multiple acoustic sensing elements are employed in a variety of beneficial ways to provide improved physiological monitoring, among other advantages. In various embodiments, sensing elements can be advantageously employed in a single sensor package, in multiple sensor packages, and at a variety of other strategic locations in the monitoring environment. According to other aspects, to compensate for skin elasticity and attachment variability, an acoustic sensor support is provided that includes one or more pressure equalization pathways. The pathways can provide an air-flow channel from the cavity defined by the sensing elements and frame to the ambient air pressure.

Abstract: A biopsy device includes a body, a needle, a cutter, a motor, a power source, a vacuum source, and a cutter translation assembly. The needle extends distally from the body and receives tissue. The cutter translates with respect to the needle to sever tissue received by the needle. The motor is disposed within the body and rotates a drive shaft in a first direction. The power source is disposed within the body and powers the motor. The vacuum source is disposed within the body and provides vacuum in at least one of the needle and the cutter. The cutter translation assembly is disposed within the body and translates the cutter proximally and distally with respect to the needle in response to rotation of the drive shaft in the first direction.

Abstract: System using on- or in-body communication technologies such as body-sound communication (BSC) or body-coupled communication (BCC) to obtain information on the body composition of a patient (e.g. water content/hydration level on bone density/joint status). The system, in a preferred embodiment, comprises a transmitter, receiver and processor connected to the receiver. The transmitter is arranged to transmit a signal through a medium (the body of the patient), the signal comprising a plurality of different frequency components and transmission technologies. The receiver is arranged to receive the signal following propagation through the said medium. The processor is arranged to generate, at a first time, one or more transfer functions from the received signal, each transfer function defining values for a predetermined signal parameter at different frequencies.

Abstract: Embodiments provide an apparatus, a system, a device, a computer program product, and a method. A method embodiment includes a method implemented in an environment that includes a person interacting with an electronic device via a user interface. The method includes monitoring at least one of a movement or a position of an appendage of the person with respect to the user interface of the device. The method also includes determining if the monitored movement or position of the appendage of the person is indicative of a risk of a repetitive injury to the person. The method further includes implementing an action facilitating a reduction of the determined indicated risk of a repetitive injury to the person.